DEANOL

Deanol = Dimethylethanolamine = DMAE 

CAS Number: 108-01-0  
EC Number: 203-542-8
Chemical formula: C4H11NO
Molar mass: 89.138 g·mol−1

Deanol is used for attention deficit-hyperactivity disorder (ADHD), Alzheimer disease, autism, and other conditions, but there is no good scientific evidence to support these uses.
Deanol was prescribed for the management of children with behavior problems and learning difficulties. 

Deanol is not an approved food additive in the U.S., nor is it an orphan drug, as some advertising suggests.
DMAE (also known as dimethylaminoethanol, dimethylethanolamine, or Deanol) is a compound sometimes used as an ingredient in lotions, creams, and other skincare products. 
Deanol is also available in dietary supplement form.

Dimethylethanolamine (DMAE or DMEA) is an organic compound with the formula (CH3)2NCH2CH2OH. 
Deanol is bifunctional, containing both a tertiary amine and primary alcohol functional groups. 

Deanol is a colorless viscous liquid. 
Deanol is used in skin care products for improving skin tone and also taken orally as a nootropic. 
Deanol is prepared by the ethoxylation of dimethylamine.

Deanol, also known as dimethylethanolamine (DMAE and DMEA respectively), is a primary alcohol. 
Deanol also goes by the names of N,N-dimethyl-2-aminoethanol, beta-dimethylaminoethyl alcohol, beta-hydroxyethyldimethylamine. 
Deanol is a transparent, pale-yellow liquid.

Uses of Deanol:
-Deanol is a precursor to other chemicals, such as the nitrogen mustard 2-dimethylaminoethyl chloride.
-The acrylate ester of Deanol is used as a flocculating agent
-Deanol is used in gas purification
-Deanols bitartrate salt is sold as a dietary supplement
-Deanol has been also used as an ingredient in skin care
-Deanol is uses in cognitive function
-Deanol is used in Mood-enhancing products.

Biochemical significance of Deanol:
Deanol is related to choline and may be a biochemical precursor to the neurotransmitter acetylcholine, although this conclusion has been disputed based on a 1977 rat experiment.
Deanol is commonly believed that dimethylaminoethanol is methylated to produce choline in the brain, but this has been shown not to be the case (in a rat experiment).

Deanol is known that dimethylaminoethanol is processed by the liver into choline; however, in a rat experiment the choline molecule is charged and cannot pass the blood–brain barrier.
In the brain, Deanol is instead bound to phospholipids in place of choline to produce phosphatidyl-dimethylaminoethanol. 
This is then incorporated into nerve membranes, increasing fluidity and permeability, and acting as an antioxidant.

Uses of Deanol:
Industrial uses:
Deanol is used as a curing agent for polyurethanes and epoxy resins. 
Deanol is also used in mass quantities for water treatment, and to some extent in the coatings industry. 
Deanol is used in the synthesis of dyestuffs, textile auxiliaries, pharmaceuticals, emulsifiers, and corrosion inhibitors. 

Deanol is also an additive to paint removers, boiler water and amino resins. 
Deanol forms a number of salts with melting points below room temperature (ionic liquids) such as N,N-dimethylethanolammonium acetate and N,N-dimethylethanolammonium octanoate, which have been used as alternatives to conventional solvents.
2-Dimethylaminoethyl chloride hydrochloride is an intermediate made from dimethylaminoethanol that is widely used for the manufacture of pharmaceuticals.

Biomedical research:
Short-term studies have shown an increase in vigilance and alertness with a positive influence on mood following administration of Deanol, vitamins, and minerals in individuals suffering from borderline emotional disturbance.
Research for ADHD has been promising, though inconclusive.
A study showed dimethylaminoethanol to decrease the average life span of aged quail.

Three other studies showed an increase in lifespan of mice.
The bitartrate salt of DMAE, i.e. 2-dimethylaminoethanol (+)-bitartrate, is sold as a dietary supplement.
It is a white powder providing 37% DMAE.

Industrial uses of Deanol:
Deanol is a precursor to other chemicals, such as the nitrogen mustard 2-dimethylaminoethyl chloride.
The acrylate ester is used as a flocculating agent.
Related compounds are used in gas purification, e.g. removal of hydrogen sulfide from sour gas streams.

Nutraceutical uses of Deanol:
The bitartrate salt of DMAE, i.e. 2-dimethylaminoethanol (+)-bitartrate, is sold as a dietary supplement.
Deanol is a white powder providing 37% DMAE.

How does Deanol work ?
Deanol is needed to build the chemical choline. 
Having more choline in the body might increase the production of acetylcholine, which is involved in brain and nervous system function.

Deanol is a compound that many people believe can positively affect mood, enhance memory, and improve brain function. 
Deanol’s also thought to have benefits for aging skin. 
Deanol is naturally produced in the body. 
Deanol’s also found in fatty fish, such as salmon, sardines, and anchovies.

Deanol is thought to work by increasing production of acetylcholine (Ach), a neurotransmitter that’s crucial for helping nerve cells send signals.
Ach helps regulate many functions controlled by the brain, including REM sleep, muscle contractions, and pain responses.

Deanol may also help prevent the buildup of a substance called beta-amyloid in the brain. 
Too much beta-amyloid has been linked to age-related decline and memory loss.
Deanol’s impact on Ach production and beta-amyloid buildup may make it beneficial for brain health, especially as we age.

USES & EFFECTIVENESS of Deanol:
Deanol is possibly Effective for:
Improving exercise performance (when used with ginseng, vitamins, and minerals).

What are the benefits of taking Deanol?
There aren’t many studies about Deanol, and most of them are older. 
However, there are a few smaller studies and anecdotal reports that suggest Deanol may have benefits.
Since it hasn’t been studied in-depth, it may make sense to have a “buyer beware” attitude.

POTENTIAL BENEFITS OF Deanol:
Reduce wrinkles and firm sagging skin. 
A randomized, clinical study reported in the American Journal of Clinical Dermatology found that a facial gel containing 3 percent Deanol was beneficial for reducing fine lines around the eyes and on the forehead when used for 16 weeks. 
The study also found it improved lip shape and fullness as well as the overall appearance of aging skin. 
A small studyTrusted Source done on humans and mice suggested Deanol may hydrate skin and improve skin appearance.

A small amount of anecdotal evidence indicates that Deanol may reduce memory loss associated with Alzheimer’s disease and dementia, but there are no studies to support this claim.
Anecdotal evidence claims Deanol may help improve athletic ability when coupled with other vitamins and supplements. 
Research is needed to support this, though.

Studies on children done during the 1950s, ’60s, and ’70s found evidence that Deanol helped reduce hyperactivity, calmed children, and helped them focus in school. 
No recent studies have been done to support or deny these findings.

Some people believe Deanol may help enhance mood and improve depression. 
A small study done in 1977 Trusted Source on people who had aging-related cognitive decline found that Deanol reduced depression, anxiety, and irritability. 
It also found that Deanol was helpful for increasing motivation and initiative.

Preferred IUPAC name for Deanol:
2-(Dimethylamino)ethan-1-ol

Other names for Deanol:
deanol, dimethylaminoethanol, dimethylaminoethanol

Deanol is commonly referred to as 2-(dimethylamino)ethanol, dimethylaminoethanol (DMAE) or dimethylethanolamine (DMEA). 
Deanol holds tertiary amine and primary alcohol groups as functional groups. 
Deanol has been used in the treatment of attention deficit-hyperactivity disorder (ADHD), Alzheimer's disease, autism, and tardive dyskinesia. 
Deanol has been also used as an ingredient in skin care, and in cognitive function- and mood-enhancing products.

CAS Number: 108-01-0  
Abbreviations: DMAE, DMEA
Beilstein Reference: 1209235
CHEBI: 271436  
ChEMBL: ChEMBL1135  
ChemSpider: 13854944  
ECHA InfoCard: 100.003.221  
EC Number: 203-542-8
KEGG: D07777  
MeSH: Deanol
PubChem CID: 7902
RTECS number: KK6125000
UNII: 2N6K9DRA24  
UN number: 2051
CompTox Dashboard (EPA): DTXSID2020505

Deanol is commonly referred to as 2-(dimethylamino)ethanol, dimethylaminoethanol (DMAE) or dimethylethanolamine (DMEA). 
Deanol holds tertiary amine and primary alcohol groups as functional groups. 
Deanol has been used in the treatment of attention deficit-hyperactivity disorder (ADHD), Alzheimer's disease, autism and tardive dyskinesia. 
Deanol has been also used as an ingredient in skin care, and in cognitive function- and mood-enhancing products.

Deanol is an inactive component hydrocortisone anti-itch cream, which is used for temporarily relieve itching associated with minor skin irritations, inflammation, and rashes due to eczema, soaps, detergents, cosmetics, seborrheic dermatitis, psoriasis. 
Deanol is also used as a food additive.

How do you use Deanol?
Deanol was once sold as a prescription drug for children with learning and behavioral problems under the name Deanol. 
Deanol was withdrawn from the market in 1983 and is no longer available as a prescribed drug.
Today, Deanol is sold as a dietary supplement in capsule and powdered form. 

Chemical formula: C4H11NO
Molar mass: 89.138 g·mol−1
Appearance    : Colourless liquid
Odor: Fishy, ammoniacal
Density: 890 mg mL−1
Melting point: −59.00 °C; −74.20 °F; 214.15 K
Boiling point: 134.1 °C; 273.3 °F; 407.2 K
log P: −0.25
Vapor pressure: 816 Pa (at 20 °C)
Acidity (pKa): 9.23 (at 20 °C) 
Basicity (pKb): 4.77 (at 20 °C)
Refractive index (nD): 1.4294

Health Benefits of Deanol:
Deanol is hypothesized to increase the production of acetylcholine (a chemical that helps nerve cells transmit signals). 
Since acetylcholine plays a key role in many brain functions, such as learning and memory, proponents claim that taking Deanol in supplement form may boost brain health by raising acetylcholine levels.

Drugs that raise acetylcholine levels have been used to treat Alzheimer's disease, so some studies have looked at Deanol as a potential Alzheimer's treatment. 
So far, however, they've failed to show any promising results.

Deanol has been used somewhat to treat attention-deficit/hyperactivity disorder (ADHD), but this use has only weak evidence behind it. 
A 2011 study on nutritional treatments stated that it "probably has a small effect."

In addition, Deanol has been looked at to boost athletic performance, elevate mood, and address symptoms of depression.
Currently, the effects of Deanol aren't scientifically well documented.

Skin Care Products:
Deanol cream, lotion, and other skin-care products are said to offer anti-aging benefits by reducing the appearance of wrinkles, dark under-eye circles, and sagging neck skin. 
While research on Deanol's effectiveness is very limited, there's some evidence that using Deanol-based products may help improve skin.

For instance, a review published in the American Journal of Clinical Dermatology states that Deanol may help to increase skin firmness and curb inflammation in the skin. 
In their analysis of previously published research, the review's authors found that Deanol may help to lessen fine wrinkles on the forehead and around the eyes and improve the overall appearance of aging skin. 
What's more, the review's authors noted that Deanol did not appear to cause common side effects such as redness, peeling, and dryness.
In a preliminary study published in Pharmazie in 2009, topically applied Deanol led to increased thickness of the epidermal and dermal skin layers (in contrast, application of formulations without Deanol increased thickness of the epidermal layer only).

Cognitive Function:
For a study published in the Journal of Alzheimer's Disease in 2012, 242 people (all of whom were diagnosed with early-stage Alzheimer's disease) took either a placebo or an oral Deanol extract known as V0191 every day for 24 weeks. 
At the study's end, there was no significant difference in cognitive function between the two groups.

The studies noted that there may have been several issues in the study design, including a relatively short treatment period, a lack of valid measures to assess the study participants, and issues with assessing changes in cognitive function over time.
There's also no evidence that oral Deanol supplements can treat depression or improve sports performance.

Deanol is a chemical that can be converted into choline. 
Choline is involved in a series of reactions that form acetylcholine, a chemical that is found in the brain and other areas of the body. 
Acetylcholine is a "neurotransmitter" that helps nerve cells communicate.

Title: Deanol
CAS Registry Number: 108-01-0
CAS Name: 2-(Dimethylamino)ethanol
Additional Names: b-dimethylaminoethyl alcohol; N,N-dimethyl-2-hydroxyethylamine
Molecular Formula: C4H11NO
Molecular Weight: 89.14
Percent Composition: C 53.90%, H 12.44%, N 15.71%, O 17.95%

Line Formula: (CH3)2NCH2CH2OH
Literature References: Prepd from equimolar amounts of ethylene oxide and dimethylamine: Knorr, Ber. 37, 3508 (1904); Hanhart, Ingold, J. Chem. Soc. 1927, 1012. 
Properties: Liquid. d420 0.8866. bp758 135°. nD20 1.43. Miscible with water, alcohol, ether.
Boiling point: bp758 135°
Index of refraction: nD20 1.43
Density: d420 0.8866
 
Derivative Type: Aceglumate
CAS Registry Number: 3342-61-8
Trademarks: Clérégil (Merck-Cl¢enot); Risatarun (Ravensberg)
Molecular Formula: C4H11NO.C7H11NO5
Molecular Weight: 278.30
Percent Composition: C 47.47%, H 7.97%, N 10.07%, O 34.49%
Literature References: Prepn: FR M2487 (1964 to Interco Fribourg), C.A. 61, 12085c (1964).
Properties: Sol in water.
 
Derivative Type: Acetamidobenzoate
CAS Registry Number: 3635-74-3
Trademarks: Deaner (3M Pharma); Pabenol (Gentili)
Molecular Formula: C4H11NO.C9H9NO3
Molecular Weight: 268.31
Percent Composition: C 58.19%, H 7.51%, N 10.44%, O 23.85%
Literature References: Prepn: GB 879259 (1957 to Riker Labs); A. Lasslo et al., J. Am. Pharm. Assoc. Sci. Ed. 48, 345 (1959).
Properties: Crystals from absolute ethanol + ethyl acetate, mp 159-161.5°. Sol in water.
Melting point: mp 159-161.5°
 
Derivative Type: Bitartrate
CAS Registry Number: 5988-51-2
Trademarks: Liparon (Finadiet)
Molecular Formula: C4H11NO.C4H6O6
Molecular Weight: 239.22
Percent Composition: C 40.17%, H 7.16%, N 5.86%, O 46.82%
Properties: Crystals, sol in water.
 
Derivative Type: Hemisuccinate
Trademarks: Tonibral (Bouchara); Rischiaril (Piam)
Molecular Formula: C4H11NO.C4H6O4
Molecular Weight: 207.22
Percent Composition: C 46.37%, H 8.27%, N 6.76%, O 38.60%
Properties: White, hygroscopic crystalline powder. Very soluble in water, ethanol; sparingly sol in chloroform, benzene.

Ten hospitalized chronic psychotic patients with symptoms of tardive dyskinesia were given deanol and placebo, each for 8 weeks following a double blind, crossover design. 
No psychotropic agents were administered during the trial. 
Improvement occurred in all patients during the first treatment phase regardless of which drug the patients received; seven patients were on deanol and three on placebo during this time. 
The possible reasons for this decrease were discussed. 
It was concluded that deanol may have contributed to the decline but that its effect on the disorder was not dramatic.

OTHER NAMES FOR DMAE:
DMAE bitartrate
deanol
2-dimethylaminoethanol
dimethylaminoethanol
dimethylaminoethanol bitartrate
dimethylethanolamine
dimethyl aminoethanol
acétamido-benzoate de déanol
benzilate de déanol
bisorcate de déanol
cyclohexylpropionate de déanol
deanol aceglumate
deanol acetamidobenzoate
deanol benzilate
deanol bisorcate
deanol cyclohexylpropionate
deanol hemisuccinate
deanol pidolate
deanol tartrate
hémisuccinate de déanol
pidolate de déanol
acéglumate de déanol

Description of Deanol: 
Deanol, being the precursor of choline, enhances the formation of central acetylcholine. 
Deanol is used in the treatment of hyperactivity in child as a stimulant and is also included in prep used as tonic and for the management of impaired mental function.

Deanol, a new drug, was used in the treatment of disorders of behavior in 108 nonepileptic and 17 epileptic children. 
In 68 per cent of the nonepileptic group, this agent proved beneficial in that the children came to act in more socially accepted patterns and learning in school improved. 
In the epileptic group it was not as beneficial as amphetamine and related drugs. 
No toxicity or significant side effects were seen at daily doses up to 200 mg.

Molecular Weight: 89.14 
XLogP3-AA: -0.4     
Hydrogen Bond Donor Count: 1     
Hydrogen Bond Acceptor Count: 2     
Rotatable Bond Count: 2     
Exact Mass: 89.084063974 
Monoisotopic Mass: 89.084063974 
Topological Polar Surface Area: 23.5 Ų     
Heavy Atom Count: 6 
Formal Charge: 0     
Complexity: 28.7 
Isotope Atom Count: 0    
Defined Atom Stereocenter Count: 0     
Undefined Atom Stereocenter Count: 0     
Defined Bond Stereocenter Count: 0     
Undefined Bond Stereocenter Count: 0     
Covalently-Bonded Unit Count: 1     
Compound Is Canonicalized: Yes    
 
Is Deanol safe?
One study on a Deanol skin care gel product concluded that it should be safe to use for most people. 
Participants applied a daily facial gel for 16 weeks and found that it tightened skin and reduced forehead lines and wrinkles. 
Some people experienced a few side effects like burning, dryness, itchiness, and stinging of the skin, but these were also reported by the placebo group.

Can Deanol be used for ADHD?
Deanol supplements are sometimes used for ADHD treatment, but there is a lack of evidence that supports their effectiveness. 
As a whole, dietary supplements are not found to be effective treatment methods.
Instead, ADHD can be managed with medication and behavioral therapy.

Purity %: 99%
Usage/Application: Ingredient in lotions and creams, Treatment of brain disorders, Chemical intermediates
Grade Standard: Industrial Grade
CAS No: 108-01-0
Synonyms: DMEA, deanol, dimethylaminoethanol, C4H11NO
Packaging Size: 180 kgs Drum
Physical State: Liquid
Color: Colorless
Odour: Fishy,ammoniacal
Molecular Weight: 89.138
Chemical Formula    : (H3C)2N CH2CH2OH
Density: 890
pH Value: 10
Melting Point: -59*C ( -74*F )
Boiling Point: 135*C ( 275*F)
Moisture: 0.2% MAX
Shelf Life: 2YEARS

Deanol, a putative acetylcholine precursor, has been used as a treatment for childhood hyperactivity for years. 
Efficacy has not been satisfactorily established, however. 
Seventy-four children referred for problems with learning, including many with hyperactivity, were screened for neurological or psychiatric illness, then given deanol, methylphenidate, or placebo in a double-blind fashion for 3 months. 
Maintenance dose for methylphenidate was 40 mg daily; for deanol, 500 mg. 
Behavior rating forms, reaction time, and a series of standard psychometric tests were given before and after treatment. 

Both drugs showed significant improvement on a number of tests; the pattern and degree of change differed slightly for the two. 
In this paradigm, deanol thus appeared to improve performance in children with learning and behavior disorders. 
The mechanism of action remains speculative; proof that deanol increases acetylcholine is scanty, and there is a theoretical basis for actually assuming an anticholinergic effect. 
Further clinical studies on deanol are indicated.

Other Name(s):
2-Dimethyl Aminoethanol
2-Dimethylaminoethanol
Acéglumate de Déanol
Acétamido-benzoate de Déanol
Benzilate de Déanol
Bisorcate de Déanol
Cyclohexylpropionate de Déanol
Déanol
Deanol Aceglumate
Deanol Acetamidobenzoate
Deanol Benzilate
Deanol Bisorcate
Deanol Cyclohexylpropionate
Deanol Hemisuccinate
Deanol Pidolate
Deanol Tartrate
Dimethylaminoethanol
Diméthylaminoéthanol
Dimethylaminoethanol Bitartrate
Dimethylethanolamine
DMAE
DMAE Bitartrate
Hémisuccinate de Déanol
Pidolate de Déanol
2-(Dimethylamino)ethanol
Deanol
N,N-Dimethylethanolamine
108-01-0
Dimethylaminoethanol
Dimethylethanolamine
2-DIMETHYLAMINOETHANOL
Norcholine
DMAE
DMEA
Bimanol
Liparon
N,N-Dimethylaminoethanol
Varesal
Propamine A
Ethanol, 2-(dimethylamino)-
(2-Hydroxyethyl)dimethylamine
Kalpur P
Dimethylmonoethanolamine
Dimethylaminoaethanol
N,N-Dimethyl-2-aminoethanol
Amietol M 21
N,N-Dimethyl-2-hydroxyethylamine
N,N-Dimethyl ethanolamine
N-Dimethylaminoethanol
2-(N,N-Dimethylamino)ethanol
Dimethyl(hydroxyethyl)amine
Texacat DME
Dimethylaethanolamin
Dimethyl(2-hydroxyethyl)amine
2-(Dimethylamino)-1-ethanol
N-(2-Hydroxyethyl)dimethylamine
N,N-Dimethyl-N-(2-hydroxyethyl)amine
2-(Dimethylamino) ethanol
(Dimethylamino)ethanol
beta-Hydroxyethyldimethylamine
2-Dimethylamino-ethanol
beta-Dimethylaminoethyl alcohol
2-(dimethylamino)ethan-1-ol
2-Dwumetyloaminoetanolu
N-(Dimethylamino)ethanol
N,N-Dimethyl-N-(beta-hydroxyethyl)amine
Tegoamin DMEA
NSC 2652
Dabco DMEA
UNII-2N6K9DRA24
Deanol [BAN]
2-Dimethylamino ethanol
N,N-Dimethyl(2-hydroxyethyl)amine
N,N'-Dimethylethanolamine
2-(dimethylamino)-ethanol
(CH3)2NCH2CH2OH
CHEMBL1135
.beta.-(Dimethylamino)ethanol
2N6K9DRA24
.beta.-Hydroxyethyldimethylamine
CHEBI:271436
Phosphatidyl-N-dimethylethanolamine
Deanol (BAN)
MFCD00002846
N,N-DIMETHYLAMINOETHANOL (DMAE)
NCGC00159413-02
Demanol
Demanyl
Tonibral
N,N-Dimethyl-N-(.beta.-hydroxyethyl)amine
DSSTox_CID_505
DSSTox_RID_75628
DSSTox_GSID_20505
N,N-Dimethylethanolamine (2-Dimethylaminoethanol)
Deanol (N,N-Dimethylethanolamine)
CAS-108-01-0
Dimethylaethanolamin [German]
Dimethylamino ethanol
Dimethylaminoaethanol [German]
CCRIS 4802
2-Dwumetyloaminoetanolu [Polish]
HSDB 1329
EINECS 203-542-8
UN2051
BRN 1209235
N,N-Dimethyl-N-ethanolamine
AI3-09209
Jeffcat DMEA
Dimethylethanoiamine
Toyocat -DMA
dimethyl ethanolamine
dimethyl-ethanolamine
Paresan (Salt/Mix)
dimethyl ethanol amine
2-dimethyamino-ethanol
n,n-dimethylethanolamin
Biocoline (Salt/Mix)
N,N dimethylaminoethanol
N,N-dimethyl-ethanolamine
N,N-dimethylamino ethanol
N,N-dimethylethanol amine
N,N-dimethylethanol-amine
2-Hydroxyethyldimethylamine
2-Dimethylaminoethanol [UN2051] [Corrosive]
EC 203-542-8
beta -(dimethylamino)ethanol
Dimethylaminoaethanol(german)
Choline chloride (Salt/Mix)
Luridin chloride (Salt/Mix)
beta -hydroxyethyldimethylamine
N,N-Dimethylethanolamine/DMEA
beta -dimethylaminoethyl alcohol
2-(N,N-dimethyl amino)ethanol
2-(N,N-dimethylamino) ethanol
DTXSID2020505
N-hydroxyethyl-N,N-dimethylamine
.beta.-Dimethylaminoethyl alcohol
2-(N,N-dimethyl amino) ethanol
Ni(1/4)OEN-Dimethylethanolamine
NSC2652
beta -(dimethylamino)ethyl alcohol
2-hydroxy-N,N-dimethylethanaminium
WLN: Q2N1 & 1
2-Dimethylaminoethanol, >=99.5%
BCP22017
CS-M3462
ZINC1641058
.beta.-(Dimethylamino)ethyl alcohol
N, N-Dimethyl(2-hydroxyethyl)amine
Tox21_113163
Tox21_201821
Tox21_302844
BDBM50060526
N,N-Dimethyl-beta -hydroxyethylamine
STL282730
Dimethylaminopropylamine Reagent Grade
AKOS000118738
N,N-Dimethyl-.beta.-hydroxyethylamine
DB13352
MCULE-7567469160
UN 2051
N, N-Dimethyl-N-(2-hydroxyethyl)amine
NCGC00159413-03
NCGC00256454-01
NCGC00259370-01
BP-13447
N,N-Dimethyl-N-(beta -hydroxyethyl)amine
DB-002821
N, N-Dimethyl-N-(beta -hydroxyethyl)amine
D0649
D07777
11064-EP2269610A2
11064-EP2270002A1
11064-EP2277848A1
11064-EP2289510A1
11064-EP2316457A1
11064-EP2316458A1
11064-EP2316825A1
11064-EP2316826A1
11064-EP2316827A1
11064-EP2316828A1
11065-EP2269610A2
11065-EP2277848A1
11065-EP2277867A2
11065-EP2280003A2
11065-EP2289510A1
11065-EP2292576A2
11065-EP2295409A1
11065-EP2298743A1
11065-EP2301937A1
11065-EP2305677A1
11065-EP2305682A1
11065-EP2305685A1
11065-EP2308840A1
11065-EP2308852A1
11065-EP2308879A1
11065-EP2311842A2
11065-EP2314590A1
11065-EP2316457A1
11065-EP2316458A1
11065-EP2316825A1
11065-EP2316826A1
11065-EP2316827A1
11065-EP2316828A1
2-Dimethylaminoethanol [UN2051] [Corrosive]
2-Dimethylaminoethanol, purum, >=98.0% (GC)
115479-EP2275420A1
115479-EP2277875A2
115479-EP2280008A2
115479-EP2295416A2
115479-EP2298748A2
115479-EP2298764A1
115479-EP2298765A1
130918-EP2286915A2
130918-EP2295433A2
130918-EP2295438A1
180727-EP2272813A2
180727-EP2275395A2
180727-EP2275414A1
180727-EP2371831A1
Q241049
2-Dimethylaminoethanol, analytical reference material
2-Dimethylaminoethanol, SAJ first grade, >=99.0%
W-108727
2-Dimethylaminoethanol, purified by redistillation, >=99.5%
108-01-0 [RN]
1209235 [Beilstein]
2-(Dimethylamino)-1-ethanol
2-(Dimethylamino)ethanol [ACD/IUPAC Name]
2-(Dimethylamino)ethanol [German] [ACD/IUPAC Name]
2-(Diméthylamino)éthanol [French] [ACD/IUPAC Name]
203-542-8 [EINECS]
2-DIMETHYLAMINOETHANOL
2-Dwumetyloaminoetanolu [Polish]
2N6K9DRA24
4-11-00-00122 [Beilstein]
Deanol [Wiki]
Dimethyl(2-hydroxyethyl)amine
Dimethyl(hydroxyethyl)amine
Dimethylaethanolamin [German]
Dimethylaminoaethanol [German]
DMAE
DMEA
Ethanol, 2-(dimethylamino)- [ACD/Index Name]
KK6125000
MFCD00002846 [MDL number]
N-(2-Hydroxyethyl)dimethylamine
N,N-Dimethyl-2-aminoethanol
N,N-Dimethyl-2-hydroxyethylamine
N,N-Dimethylethanolamine
N,N-Dimethyl-N-(2-hydroxyethyl)amine
N,N-Dimethyl-N-(β-hydroxyethyl)amine
UNII-2N6K9DRA24
β-Dimethylaminoethyl alcohol
β-Hydroxyethyldimethylamine
(2-Hydroxyethyl)dimethylamine
(CH3)2NCH2CH2OH
(Dimethylamino)ethanol
116134-09-9 alternate RN [RN]
2-(Dimethylamino) ethanol
2-(dimethylamino)ethan-1-ol
2-(Dimethylamino)-ethanol
2-(N,N-Dimethylamino)ethanol
2-Dimethylamino ethanol
2-Dimethylamino-ethanol
Amietol M 21 [Trade name]
Bimanol [Trade name]
Demanol [Trade name]
Dimethylaminoethanol [Wiki]
Dimethylethanoiamine
Dimethylethanolamine [Wiki]
Dimethylmonoethanolamine
Kalpur P [Trade name]
Liparon [Trade name]
N-(Dimethylamino)ethanol
N, N-Dimethylethanolamine
N,N-Dimethyl ethanolamine
N,N-Dimethyl(2-hydroxyethyl)amine
N,N-dimethylaminoethanol
N,N'-Dimethylethanolamine
N,N-Dimethyl-N-(β -hydroxyethyl)amine
N,N-Dimethyl-N-(β-hydroxyethyl)amine
N,N-Dimethyl-N-ethanolamine
N,N-Dimethyl-N-ethanolamine.
N,N-Dimethyl-β -hydroxyethylamine
N,N-Dimethyl-β-hydroxyethylamine
N-Benzyloxycarbonyl-L-tyrosine
N-dimethyl aminoethanol
N-Dimethylaminoethanol
Norcholine [Trade name]
Propamine A [Trade name]
Q2N1 & 1 [WLN]
Texacat DME [Trade name]
UN 2051
Varesal [Trade name]
β -(dimethylamino)ethanol
β -(dimethylamino)ethyl alcohol
β -dimethylaminoethyl alcohol
β -hydroxyethyldimethylamine
β-(Dimethylamino)ethanol
β-(Dimethylamino)ethyl alcohol
β-Dimethylaminoethyl alcohol
β-Hydroxyethyldimethylamine
2-DIMETHYLAMINO-ETHANOL
2-dimethylaminoethanol
2-DIMETHYLAMINOETHANOL
2-dimethylaminoethanol
2-dimethylaminoethanol; N,N-dimethylethanolamine

Translated names
2-(dimethylamino)ethan-1-ol (cs)
2-(dimetylamino)etanol (sk)
2-(dimetyloamino)etanol (pl)
2-dimethylaminoethanol (da)
2-Dimethylaminoethanol (de)
2-dimethylaminoethanol (nl)
2-dimetil-aminoetanol (hr)
2-dimetilaminoetanol (es)
2-dimetilaminoetanol (hu)
2-dimetilaminoetanol (pt)
2-dimetilaminoetanol (ro)
2-dimetilaminoetanol (sl)
2-dimetilaminoetanolis (lt)
2-dimetilaminoetanolo (it)
2-dimetilaminoetanols (lv)
2-dimetylaminoetanol (no)
2-dimetylaminoetanol (sv)
2-dimetyyliaminoetanoli (fi)
2-dimetüülaminoetanool (et)
2-diméthylaminoéthanol N,N-diméthyléthanolamine (fr)
2-διμεθυλαμινοαιθανόλ (el)
2-диметиламиноетанол (bg)
<I>N,N</I>-dimetil-etanolamin (hr)
N,N-dimethylethanolamin (cs)
N,N-Dimethylethanolamin (de)
N,N-dimetiletanolamin (hu)
N,N-dimetiletanolamin (sl)
N,N-dimetiletanolamina (ro)
N,N-dimetiletanolaminas (lt)
N,N-dimetiletanolamīns (lv)
N,N-dimetyletanolamín (sk)
N,N-dimetyloetanoloamina (pl)
N,N-dimetüületanoolamiin (et)
N,N-диметилетаноламин (bg)

IUPAC names
2- Dimethylaminoethanol
2-(Dimethylamino) ethanol
2-(dimethylamino)-ethanol
2-(dimethylamino)ethan-1-ol
2-(Dimethylamino)ethanol
2-(dimethylamino)ethanol
2-(dimethylamino)ethanol
2-Dimethylaminoethanol
2-dimethylaminoethanol
2-Dimethylaminoethanol
2-dimethylaminoethanol
2-dimethylaminoethanol, DMAE
2-dimethylaminoethanol;
2-dimethylaminoethanol; N,N-dimethylethanolamine
Dimethylaminoethanol
DIMETHYLAMINOETHANOL
Dimethylaminoethanol
Dimethylethanolamine
DMAE
DMAE - CM0564B
N,N-Dimethylethanolamine
N,N-dimethylethanolamine
 

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